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Intramolecular double Michael reaction. Part II. Synthesis of isoatisirene type compound
Authors:Masataka Ihara  Masahiro Toyota  Keiichiro Fukumoto  Tetsuji Kametani
Affiliation:1. Pharmaceutical Institute, Tohoku University, Aobayama, Sendai 980, Japan;2. Institute of Medicinal Chemistry, Hoshi University, Ebara 2-4-41, Shinagawa-ku, Tokyo 142, Japan
Abstract:Intramolecular double Michael reaction of the α,β-unsaturated enone ester (16), prepared from the dienone (5), stereoselectively gave the tetracyclic product (17), which was converted into the isoatisirene type compound (20).
Keywords:
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